Endomat Tubing Set (2020-08-14)

Starting date:

August 14, 2020

Posting date:

August 28, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-73793

Last updated:
2020-08-28

• 
  Reason
• 
  Affected products

Affected Products

Endomat Tubing Set

Reason

The affected tubing kits contain a component, which codes the application of the kit and enables the pump pressure and flow settings.

At the affected batch numbers, there may have been code components  from a different application assembled. If operated according to the IFU, the pump will display a warning if an affected set is mounted.

Affected products